DE69232002T2 - Immunoassays unter Verwendung von markierten Hapten-Analogen - Google Patents
Immunoassays unter Verwendung von markierten Hapten-AnalogenInfo
- Publication number
- DE69232002T2 DE69232002T2 DE69232002T DE69232002T DE69232002T2 DE 69232002 T2 DE69232002 T2 DE 69232002T2 DE 69232002 T DE69232002 T DE 69232002T DE 69232002 T DE69232002 T DE 69232002T DE 69232002 T2 DE69232002 T2 DE 69232002T2
- Authority
- DE
- Germany
- Prior art keywords
- label
- analogue
- immunoassay
- groups
- phenobarbital
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
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- DDBREPKUVSBGFI-UHFFFAOYSA-N phenobarbital Chemical group C=1C=CC=CC=1C1(CC)C(=O)NC(=O)NC1=O DDBREPKUVSBGFI-UHFFFAOYSA-N 0.000 claims description 33
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- 238000000034 method Methods 0.000 claims description 20
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- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical class [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 239000012491 analyte Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- TZSLWQVJSTVTMP-UHFFFAOYSA-N benzyl 2,4-diaminobutanoate Chemical compound NCCC(N)C(=O)OCC1=CC=CC=C1 TZSLWQVJSTVTMP-UHFFFAOYSA-N 0.000 description 1
- OXZSVNMAOOMREC-UHFFFAOYSA-N benzyl 4-[5-(2,5-dioxo-4,4-diphenylimidazolidin-1-yl)pentanoyl]piperazine-1-carboxylate Chemical compound C1CN(C(=O)OCC=2C=CC=CC=2)CCN1C(=O)CCCCN(C1=O)C(=O)NC1(C=1C=CC=CC=1)C1=CC=CC=C1 OXZSVNMAOOMREC-UHFFFAOYSA-N 0.000 description 1
- CZWYESODPJCZSY-UHFFFAOYSA-N benzyl 4-[5-(5-ethyl-2,4,6-trioxo-5-phenyl-1,3-diazinan-1-yl)pentanoyl]piperazine-1-carboxylate Chemical compound O=C1C(CC)(C=2C=CC=CC=2)C(=O)NC(=O)N1CCCCC(=O)N(CC1)CCN1C(=O)OCC1=CC=CC=C1 CZWYESODPJCZSY-UHFFFAOYSA-N 0.000 description 1
- JXWABCYGGVHAHB-UHFFFAOYSA-N benzyl n-(3-aminopropyl)carbamate Chemical compound NCCCNC(=O)OCC1=CC=CC=C1 JXWABCYGGVHAHB-UHFFFAOYSA-N 0.000 description 1
- FPZYKXIQAFSJBL-UHFFFAOYSA-N benzyl n-[3-[5-(5-ethyl-2,4,6-trioxo-5-phenyl-1,3-diazinan-1-yl)pentanoylamino]propyl]carbamate Chemical compound O=C1C(CC)(C=2C=CC=CC=2)C(=O)NC(=O)N1CCCCC(=O)NCCCNC(=O)OCC1=CC=CC=C1 FPZYKXIQAFSJBL-UHFFFAOYSA-N 0.000 description 1
- OLFPNNKQTLQAEK-UHFFFAOYSA-N benzyl n-[6-[5-(2,5-dioxo-4,4-diphenylimidazolidin-1-yl)pentanoylamino]hexyl]carbamate Chemical compound C=1C=CC=CC=1COC(=O)NCCCCCCNC(=O)CCCCN(C1=O)C(=O)NC1(C=1C=CC=CC=1)C1=CC=CC=C1 OLFPNNKQTLQAEK-UHFFFAOYSA-N 0.000 description 1
- 239000013060 biological fluid Substances 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 229910052681 coesite Inorganic materials 0.000 description 1
- 230000002860 competitive effect Effects 0.000 description 1
- 230000021615 conjugation Effects 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 229910052906 cristobalite Inorganic materials 0.000 description 1
- 239000013058 crude material Substances 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000012992 electron transfer agent Substances 0.000 description 1
- 239000002532 enzyme inhibitor Substances 0.000 description 1
- 239000000174 gluconic acid Substances 0.000 description 1
- 235000012208 gluconic acid Nutrition 0.000 description 1
- SYECJBOWSGTPLU-UHFFFAOYSA-N hexane-1,1-diamine Chemical compound CCCCCC(N)N SYECJBOWSGTPLU-UHFFFAOYSA-N 0.000 description 1
- 229940088597 hormone Drugs 0.000 description 1
- 239000005556 hormone Substances 0.000 description 1
- 150000002440 hydroxy compounds Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 230000008105 immune reaction Effects 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- XMBWDFGMSWQBCA-RNFDNDRNSA-M iodine-131(1-) Chemical compound [131I-] XMBWDFGMSWQBCA-RNFDNDRNSA-M 0.000 description 1
- UBMRMPDCVDGINV-UHFFFAOYSA-N methyl 5-(5-ethyl-2,4,6-trioxo-5-phenyl-1,3-diazinan-1-yl)pentanoate Chemical compound C=1C=CC=CC=1C1(CC)C(O)=NC(=O)N(CCCCC(=O)OC)C1=O UBMRMPDCVDGINV-UHFFFAOYSA-N 0.000 description 1
- RAVVJKCSZXAIQP-UHFFFAOYSA-N methyl 5-bromopentanoate Chemical compound COC(=O)CCCCBr RAVVJKCSZXAIQP-UHFFFAOYSA-N 0.000 description 1
- BISVVKSTXIKDMH-UHFFFAOYSA-N n-(3-aminopropyl)-5-(5-ethyl-2,4,6-trioxo-5-phenyl-1,3-diazinan-1-yl)pentanamide;hydrobromide Chemical compound Br.C=1C=CC=CC=1C1(CC)C(=O)NC(=O)N(CCCCC(=O)NCCCN)C1=O BISVVKSTXIKDMH-UHFFFAOYSA-N 0.000 description 1
- AIQODGUCINLCAT-UHFFFAOYSA-N n-(6-aminohexyl)-5-(2,5-dioxo-4,4-diphenylimidazolidin-1-yl)pentanamide Chemical compound O=C1N(CCCCC(=O)NCCCCCCN)C(=O)NC1(C=1C=CC=CC=1)C1=CC=CC=C1 AIQODGUCINLCAT-UHFFFAOYSA-N 0.000 description 1
- 239000004081 narcotic agent Substances 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- 230000000269 nucleophilic effect Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 230000003617 peroxidasic effect Effects 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000012857 radioactive material Substances 0.000 description 1
- 238000003127 radioimmunoassay Methods 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 229910052682 stishovite Inorganic materials 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 229940124597 therapeutic agent Drugs 0.000 description 1
- 150000007970 thio esters Chemical class 0.000 description 1
- 229910052905 tridymite Inorganic materials 0.000 description 1
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 1
- 238000003260 vortexing Methods 0.000 description 1
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
- G01N33/531—Production of immunochemical test materials
- G01N33/532—Production of labelled immunochemicals
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
- G01N33/543—Immunoassay; Biospecific binding assay; Materials therefor with an insoluble carrier for immobilising immunochemicals
- G01N33/54366—Apparatus specially adapted for solid-phase testing
- G01N33/54386—Analytical elements
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/94—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving narcotics or drugs or pharmaceuticals, neurotransmitters or associated receptors
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/94—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving narcotics or drugs or pharmaceuticals, neurotransmitters or associated receptors
- G01N33/948—Sedatives, e.g. cannabinoids, barbiturates
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S436/00—Chemistry: analytical and immunological testing
- Y10S436/815—Test for named compound or class of compounds
- Y10S436/816—Alkaloids, amphetamines, and barbiturates
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Molecular Biology (AREA)
- Hematology (AREA)
- Chemical & Material Sciences (AREA)
- Urology & Nephrology (AREA)
- Biomedical Technology (AREA)
- Microbiology (AREA)
- Pathology (AREA)
- Biotechnology (AREA)
- Cell Biology (AREA)
- General Physics & Mathematics (AREA)
- General Health & Medical Sciences (AREA)
- Food Science & Technology (AREA)
- Medicinal Chemistry (AREA)
- Physics & Mathematics (AREA)
- Analytical Chemistry (AREA)
- Biochemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Anesthesiology (AREA)
- Plural Heterocyclic Compounds (AREA)
- Steroid Compounds (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US71232891A | 1991-06-07 | 1991-06-07 | |
US85143692A | 1992-03-16 | 1992-03-16 |
Publications (2)
Publication Number | Publication Date |
---|---|
DE69232002D1 DE69232002D1 (de) | 2001-09-20 |
DE69232002T2 true DE69232002T2 (de) | 2002-06-06 |
Family
ID=27108808
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE69232002T Expired - Lifetime DE69232002T2 (de) | 1991-06-07 | 1992-06-02 | Immunoassays unter Verwendung von markierten Hapten-Analogen |
Country Status (5)
Country | Link |
---|---|
US (1) | US5601994A (fr) |
EP (1) | EP0517327B1 (fr) |
JP (1) | JP3190730B2 (fr) |
AT (1) | ATE204385T1 (fr) |
DE (1) | DE69232002T2 (fr) |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2960628B2 (ja) * | 1992-06-26 | 1999-10-12 | イーストマン コダック カンパニー | 標識サイロニンハプテン類似体を用いたイムノアッセイ |
ATE161962T1 (de) * | 1992-08-07 | 1998-01-15 | Johnson & Johnson Clin Diag | Immunoassays unter verwendung von, mit meerrettich-peroxidase markierten carbamazepin- analogen |
US5565326A (en) | 1994-05-31 | 1996-10-15 | Johnson & Johnson Clinical Diagnostics, Inc. | Separation-free specific binding assays using anti-inhibitor antibodies |
US5650324A (en) | 1994-05-31 | 1997-07-22 | Johnson & Johnson Clinical Diagnostics, Inc. | Inhibitor and anti-inhibitor monoclonal antibodies specific for horseradish peroxidase |
US5589344A (en) * | 1994-06-15 | 1996-12-31 | Johnson & Johnson Clinical Diagnostics, Inc. | Test kit and method for competitive specific binding assay |
AU697785B2 (en) | 1994-07-19 | 1998-10-15 | Johnson & Johnson Clinical Diagnostics, Inc. | Analytical element,composition and method using modified apo-horseradish peroxidase |
ES2167278B1 (es) * | 2000-10-24 | 2003-08-16 | Univ Murcia | Enzima con actividad peroxidasa aislada de la alcachofa (cynara scolymus, l.) procedimiento para su aislamiento y purificacion y aplicaciones. |
US8133743B2 (en) | 2007-10-19 | 2012-03-13 | Roche Diagnostics Operations, Inc. | Phenobarbital derivatives useful in immunoassay |
CN104736561B (zh) | 2012-08-21 | 2018-06-12 | 詹森药业有限公司 | 帕潘立酮的抗体及其用途 |
AU2013305938B2 (en) | 2012-08-21 | 2017-08-17 | Saladax Biomedical Inc. | Antibodies to paliperidone haptens and use thereof |
CN104736565B (zh) | 2012-08-21 | 2019-03-12 | 詹森药业有限公司 | 利培酮半抗原的抗体及其用途 |
JP6389177B2 (ja) | 2012-08-21 | 2018-09-12 | ヤンセン ファーマシューティカ エヌ.ベー. | オランザピンハプテンに対する抗体及びその使用 |
CN107043424B (zh) | 2012-08-21 | 2021-03-16 | 詹森药业有限公司 | 利培酮的抗体及其用途 |
JP6949025B2 (ja) | 2015-12-17 | 2021-10-13 | ヤンセン ファーマシューティカ エヌ.ベー. | リスペリドンに対する抗体及びその使用 |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3875011A (en) * | 1972-11-06 | 1975-04-01 | Syva Co | Enzyme immunoassays with glucose-6-phosphate dehydrogenase |
US4065354A (en) * | 1974-10-10 | 1977-12-27 | Syva Company | Lysozyme conjugates for enzyme immunoassays |
US4213964A (en) * | 1978-12-07 | 1980-07-22 | Miles Laboratories, Inc. | Diphenylhydantoin antibodies |
IL59065A0 (en) * | 1979-01-18 | 1980-05-30 | Beecham Group Ltd | Hydantoin derivatives,their preparation pharmaceutical compositons containing them |
US4404366A (en) * | 1980-05-06 | 1983-09-13 | Miles Laboratories, Inc. | Beta-galactosyl-umbelliferone-labeled hapten conjugates |
NZ199629A (en) * | 1981-02-17 | 1984-11-09 | Abbott Lab | Fluorescent polarisation immunoassay and certain substituted carboxy fluoresceins |
US4378428A (en) * | 1981-03-30 | 1983-03-29 | Baker Instruments Corporation | Method for carrying out non-isotopic immunoassays, labeled analytes and kits for use in such assays |
US4447529A (en) * | 1981-07-06 | 1984-05-08 | Miles Laboratories, Inc. | Preparing homogeneous specific binding assay element to avoid premature reaction |
US4752568A (en) * | 1986-01-13 | 1988-06-21 | Eastman Kodak Company | Labeled hydantoin conjugate and its use in analytical element and immunoassays |
CA1300499C (fr) * | 1987-08-03 | 1992-05-12 | Susan J. Danielson | Reactif insoluble dans l'eau, elements qui en contiennent et methode d'utilisation |
DK0386644T3 (da) * | 1989-03-10 | 1997-10-13 | Hoffmann La Roche | Reagenser til bestemmelse af lægemidler |
US5096838A (en) * | 1989-11-27 | 1992-03-17 | Abbott Laboratories | Barbiturate assay compositions and methods |
US5162219A (en) * | 1990-06-18 | 1992-11-10 | Eastman Kodak Company | Preparation of amine-enriched proteins having an increased isoelectric point |
-
1992
- 1992-06-02 DE DE69232002T patent/DE69232002T2/de not_active Expired - Lifetime
- 1992-06-02 EP EP92201582A patent/EP0517327B1/fr not_active Expired - Lifetime
- 1992-06-02 AT AT92201582T patent/ATE204385T1/de active
- 1992-06-05 JP JP14600792A patent/JP3190730B2/ja not_active Expired - Fee Related
-
1994
- 1994-04-28 US US08/235,114 patent/US5601994A/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
EP0517327A3 (en) | 1993-05-05 |
JPH0627108A (ja) | 1994-02-04 |
ATE204385T1 (de) | 2001-09-15 |
EP0517327B1 (fr) | 2001-08-16 |
JP3190730B2 (ja) | 2001-07-23 |
US5601994A (en) | 1997-02-11 |
EP0517327A2 (fr) | 1992-12-09 |
DE69232002D1 (de) | 2001-09-20 |
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